Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41598-018-25665-5
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dc.titleConcentration-dependent protein loading of extracellular vesicles released by Histoplasma capsulatum after antibody treatment and its modulatory action upon macrophages
dc.contributor.authorBaltazar, L.M
dc.contributor.authorZamith-Miranda, D
dc.contributor.authorBurnet, M.C
dc.contributor.authorChoi, H
dc.contributor.authorNimrichter, L
dc.contributor.authorNakayasu, E.S
dc.contributor.authorNosanchuk, J.D
dc.date.accessioned2020-09-09T03:03:05Z
dc.date.available2020-09-09T03:03:05Z
dc.date.issued2018
dc.identifier.citationBaltazar, L.M, Zamith-Miranda, D, Burnet, M.C, Choi, H, Nimrichter, L, Nakayasu, E.S, Nosanchuk, J.D (2018). Concentration-dependent protein loading of extracellular vesicles released by Histoplasma capsulatum after antibody treatment and its modulatory action upon macrophages. Scientific Reports 8 (1) : 8065. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-018-25665-5
dc.identifier.issn20452322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/175022
dc.description.abstractDiverse pathogenic fungi secrete extracellular vesicles (EV) that contain macromolecules, including virulence factors that can modulate the host immune response. We recently demonstrated that the binding of monoclonal antibodies (mAb) modulates how Histoplasma capsulatum load and releases its extracellular vesicles (EV). In the present paper, we addressed a concentration-dependent impact on the fungus' EV loading and release with different mAb, as well as the pathophysiological role of these EV during the host-pathogen interaction. We found that the mAbs differentially regulate EV content in concentration-dependent and independent manners. Enzymatic assays demonstrated that laccase activity in EV from H. capsulatum opsonized with 6B7 was reduced, but urease activity was not altered. The uptake of H. capsulatum by macrophages pre-treated with EV, presented an antibody concentration-dependent phenotype. The intracellular killing of yeast cells was potently inhibited in macrophages pre-treated with EV from 7B6 (non-protective) mAb-opsonized H. capsulatum and this inhibition was associated with a decrease in the reactive-oxygen species generated by these macrophages. In summary, our findings show that opsonization quantitatively and qualitatively modifies H. capsulatum EV load and secretion leading to distinct effects on the host's immune effector mechanisms, supporting the hypothesis that EV sorting and secretion are dynamic mechanisms for a fine-tuned response by fungal cells. © 2018 The Author(s).
dc.sourceUnpaywall 20200831
dc.subjectchaperonin 60
dc.subjectfungus antibody
dc.subjectHspd1 protein, mouse
dc.subjectmitochondrial protein
dc.subjectmonoclonal antibody
dc.subjectproteome
dc.subjectanimal
dc.subjectBagg albino mouse
dc.subjectcell culture
dc.subjectcytology
dc.subjectexosome
dc.subjectfemale
dc.subjectHistoplasma
dc.subjecthistoplasmosis
dc.subjecthost pathogen interaction
dc.subjectimmunology
dc.subjectmacrophage
dc.subjectmetabolism
dc.subjectmicrobiology
dc.subjectmortality
dc.subjectmouse
dc.subjectpathogenicity
dc.subjectphagocytosis
dc.subjectAnimals
dc.subjectAntibodies, Fungal
dc.subjectAntibodies, Monoclonal
dc.subjectCells, Cultured
dc.subjectChaperonin 60
dc.subjectExtracellular Vesicles
dc.subjectFemale
dc.subjectHistoplasma
dc.subjectHistoplasmosis
dc.subjectHost-Pathogen Interactions
dc.subjectMacrophages
dc.subjectMice
dc.subjectMice, Inbred BALB C
dc.subjectMitochondrial Proteins
dc.subjectPhagocytosis
dc.subjectProteome
dc.typeArticle
dc.contributor.departmentSAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
dc.description.doi10.1038/s41598-018-25665-5
dc.description.sourcetitleScientific Reports
dc.description.volume8
dc.description.issue1
dc.description.page8065
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